- OMIM ID
-
208920
- OMIM term:
- ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH
- Alternative terms:
-
ATAXIA-OCULOMOTOR APRAXIA SYNDROME; AOA
ATAXIA-OCULOMOTOR APRAXIA 1; AOA1
ATAXIA-TELANGIECTASIA-LIKE SYNDROME
CEREBELLAR ATAXIA, EARLY-ONSET, WITH HYPOALBUMINEMIA; EOCA-HA ATAXIA, ADULT-ONSET, WITH OCULOMOTOR APRAXIA, INCLUDED
- (∗) Location:
- 9p21.1
- (†) Associated OMIM genes:
- APTX
- (‡) Associated MGI genes:
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